Bleeding Disorders Overview
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Questions and Answers

What is a common clinical manifestation of platelet defects?

  • Subcutaneous hematomas
  • Hemorrhage into joint spaces
  • Petechiae in clusters (correct)
  • Deep muscle bleeding
  • What is one primary cause of increased platelet levels in response to bleeding?

  • Loss of platelet pooling in the spleen (correct)
  • Decreased platelet production
  • Formation of blood clots
  • Increased platelet destruction
  • Which nursing action is essential for patients with bleeding disorders?

  • Encouraging contact sports
  • Educating about the signs of bleeding (correct)
  • Promoting high-impact activities
  • Monitoring for signs of infection
  • How should bleeding caused by coagulation factor defects be characterized?

    <p>Deep bleeding into soft tissues</p> Signup and view all the answers

    Which therapeutic agent can inhibit bleeding mechanisms in patients?

    <p>Aminocaproic acid (Amicar)</p> Signup and view all the answers

    What is a typical precaution patients with bleeding disorders should take?

    <p>Avoiding activities that increase bleeding risk</p> Signup and view all the answers

    What type of bleeding is less common in patients with coagulation factor defects?

    <p>Petechiae on the skin</p> Signup and view all the answers

    What is a reactive response by the bone marrow to bleeding?

    <p>Increased platelet production (thrombopoiesis)</p> Signup and view all the answers

    What medical management strategy should be implemented when platelet dysfunction is caused by medication?

    <p>Stop the medication if possible</p> Signup and view all the answers

    Which condition is indicated by an elevated PT with normal aPTT and platelet count?

    <p>Factor VII deficiency</p> Signup and view all the answers

    Which symptom is common in patients with platelet dysfunction?

    <p>Ecchymoses on extremities</p> Signup and view all the answers

    What is a potential effect of NSAIDs on platelet function compared to aspirin?

    <p>Shorter inhibition of platelet function</p> Signup and view all the answers

    What role do antifibrinolytic agents play in managing marked platelet dysfunction?

    <p>Prevent significant bleeding after procedures</p> Signup and view all the answers

    Which of the following is NOT a cause of platelet dysfunction?

    <p>High blood pressure</p> Signup and view all the answers

    What is an important nursing instruction for patients with platelet dysfunction?

    <p>Avoid substances that diminish platelet function</p> Signup and view all the answers

    Which medication can be used to improve hemostasis in some patients with platelet dysfunction?

    <p>Desmopressin (DDAVP)</p> Signup and view all the answers

    What treatment option is typically used for Immune Thrombocytopenic Purpura (ITP)?

    <p>Corticosteroids</p> Signup and view all the answers

    Which is a common clinical manifestation of bleeding disorders related to platelet dysfunction?

    <p>Petechiae and purpura</p> Signup and view all the answers

    What is a primary cause of bleeding disorders due to platelet abnormalities?

    <p>Leukemia</p> Signup and view all the answers

    Which condition can lead to lymphocyte depletion and potentially increase the risk of opportunistic infections?

    <p>Human immunodeficiency virus (HIV)</p> Signup and view all the answers

    What should a patient with neutropenia do to protect themselves from infections?

    <p>Avoid crowded places</p> Signup and view all the answers

    Which of the following is NOT a potential cause of bleeding disorders?

    <p>Cardiovascular disease</p> Signup and view all the answers

    What is a typical recommendation for fluid intake for patients at risk for infection?

    <p>3000 mL daily</p> Signup and view all the answers

    In cases of severe lymphopenia, what type of infections are most commonly seen?

    <p>Opportunistic infections</p> Signup and view all the answers

    Study Notes

    Bleeding Disorders

    • Bleeding disorders occur due to ineffective hemostatic mechanisms leading to bleeding.
    • Trauma can provoke bleeding, and it may occur spontaneously in some cases.
    • Bleeding can be localized if the source is vascular abnormalities
    • Bleeding can be systemic if the cause is platelet or coagulation factor abnormalities.
    • Patients can have defects in multiple hemostatic mechanisms simultaneously.
    • The bone marrow can be stimulated to increase platelet production as a response to bleeding.
    • Platelet increases may not be due to increased production, but to loss of platelet pooling in the spleen.

    Clinical Manifestations

    • Bleeding disorder symptoms vary with the type of defect.
    • Vascular system abnormalities cause local bleeding, primarily in the skin.
    • Platelet defects lead to petechiae formation, often clustered.
    • Bleeding from platelet disorders can be severe.
    • Coagulation factor defects don't typically cause superficial bleeding due to intact primary hemostatic mechanisms.
    • Bleeding with coagulation factor defects occurs deeper in the body (e.g., subcutaneous or intramuscular hematomas, hemorrhage into joint spaces).

    Medical Management

    • Management depends on the underlying cause.
    • Transfusions of blood products may be required.
    • Hemostatic agents such as aminocaproic acid (Amicar) can inhibit fibrinolysis.
    • Patients needing invasive procedures (like tooth extraction) may require pre-procedure transfusions to minimize bleeding risk.

    Nursing Management

    • Educate patients about self-monitoring for signs of bleeding.
    • Emphasize avoiding activities that increase bleeding risk (e.g., contact sports).
    • Regularly inspect the skin for petechiae and ecchymoses, as well as the nose and gums for bleeding.
    • Hospitalized patients with severe bleeding are monitored for occult blood in drainage and excreta (feces, urine, emesis, and gastric drainage).

    Platelet Defects

    • Bleeding can range from mild to severe.
    • Elevated Prothrombin Time (PT) with normal Activated Partial Thromboplastin Time (aPTT) and platelet count can indicate factor VII deficiency.
    • Elevated Partial Thromboplastin Time (PTT) with normal PT and platelet count might suggest hemophilia or von Willebrand disease (vWD).
    • Ecchymoses are common, especially on extremities.
    • Patients with platelet dysfunction have increased risk for significant bleeding after trauma or invasive procedures.

    Platelet Defects: Medical Management

    • If medication causes platelet dysfunction, discontinue use if possible.
    • Transfusion of normal platelets before invasive procedures can prevent bleeding if platelet dysfunction is severe.
    • Antifibrinolytic agents (e.g., aminocaproic acid) may be required to prevent significant bleeding after procedures.
    • Desmopressin (DDAVP) can shorten bleeding duration and improve hemostasis in certain cases.

    Platelet Defects: Nursing Management

    • Advise patients to avoid substances that impair platelet function (e.g., some OTC medications, herbal therapies, nutritional supplements, alcohol).
    • Patients with platelet dysfunction should inform all healthcare providers (including dentists) about their condition before any invasive procedures for appropriate bleeding prevention measures.
    • Maintaining good oral hygiene is vital to minimize gingival bleeding.

    Hemophilia

    • Hemophilia A results from a genetic defect leading to deficient or defective factor VIII.

    Neutropenia: The Patient at Risk for Infection

    • Educate patients and caregivers to avoid individuals with infections and crowds.
    • Encourage deep breathing and incentive spirometer use every 4 hours while awake (if mobility is restricted).
    • Provide sufficient lubrication during sexual intercourse with gentle vaginal manipulation, avoid anal intercourse.
    • Teach patients to recognize and monitor for signs of infection.
    • Instruct patients on reporting signs of infection, and appropriate actions if infection occurs.

    Lymphopenia

    • Lymphocyte count below 1500/mm3.
    • Caused by ionizing radiation, long-term corticosteroid use, uremia, infections (particularly viral), certain neoplasms (e.g., breast and lung cancers, advanced Hodgkin disease), and some protein-losing enteropathies.
    • Mild lymphopenia often has no consequences.
    • Severe lymphopenia can lead to bacterial infections (due to low B-lymphocytes) or opportunistic infections (due to low T-lymphocytes).

    T Cell Lymphocyte Depletion

    • T cell depletion is commonly due to viral infections like HIV.

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    Description

    This quiz explores the key concepts surrounding bleeding disorders, including their mechanisms and clinical manifestations. It covers topics like hemostatic pathways, the impact of trauma, and symptoms related to various defects. Test your understanding of how these disorders affect patients and their treatment options.

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